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Details

Stereochemistry ACHIRAL
Molecular Formula C4H5N
Molecular Weight 67.0892
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHACRYLONITRILE

SMILES

CC(=C)C#N

InChI

InChIKey=GYCMBHHDWRMZGG-UHFFFAOYSA-N
InChI=1S/C4H5N/c1-4(2)3-5/h1H2,2H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Role of cytochrome P-450 2E1 in methacrylonitrile metabolism and disposition.
1999 May
Comparative xenobiotic metabolism between Tg.AC and p53+/- genetically altered mice and their respective wild types.
2001 May
Brain lipid peroxidation and antioxidant status after acute methacrylonitrile intoxication.
2005
Enantioselective addition of secondary phosphines to methacrylonitrile: catalysis and mechanism.
2005 Dec 7
Directed organic grafting on locally doped silicon substrates.
2005 Jan
Comparative metabolism of methacrylonitrile and acrylonitrile to cyanide using cytochrome P4502E1 and microsomal epoxide hydrolase-null mice.
2005 Jun 1
Half-sandwich rhodium (and iridium) complexes as enantioselective catalysts for the 1,3-dipolar cycloaddition of 3,4-dihydroisoquinoline N-oxide to methacrylonitrile.
2007
Investigation of xenobiotics metabolism, genotoxicity, and carcinogenicity using Cyp2e1(-/-) mice.
2007 Oct
Effect of methacrylonitrile on membrane bound enzymes of rat brain.
2007 Oct-Dec
Effect of caffeine and alcohol on the toxicity and metabolism of methacrylonitrile in male Sprague-Dawley rats.
2007-2008
Novel catalytic activity of nitrile hydratase from Rhodococcus sp. N771.
2008 Aug
Magneto-responsive organogels prepared through surface-initiated atom transfer radical polymerization on iron nanoparticles.
2009 Jan
Elementary reactions and their role in gas-phase prebiotic chemistry.
2009 May 19
Comparative investigations of genotoxic activity of five nitriles in the comet assay and the Ames test.
2009 Sep 30
Cloning and functional expression of a nitrile hydratase (NHase) from Rhodococcus equi TG328-2 in Escherichia coli, its purification and biochemical characterisation.
2010 Feb
Photocycloaddition of enynones (4-acylbut-1-en-3-ynes) to alkenes.
2010 Feb 19
Patents
Name Type Language
METHACRYLONITRILE
MI  
Systematic Name English
.ALPHA.-METHYLACRYLONITRILE
Systematic Name English
METHYLACRYLONITRILE [HSDB]
Common Name English
ISOBUTENENITRILE
Systematic Name English
NSC-24145
Code English
ISOPROPENE CYANIDE
Common Name English
2-METHYL-2-PROPENENITRILE
Systematic Name English
2-CYANO-1-PROPENE
Systematic Name English
ISOPROPENYLNITRILE
Common Name English
METHACRYLONITRILE [MI]
Common Name English
Code System Code Type Description
MERCK INDEX
m7284
Created by admin on Fri Dec 15 18:25:55 GMT 2023 , Edited by admin on Fri Dec 15 18:25:55 GMT 2023
PRIMARY Merck Index
FDA UNII
04S4K38612
Created by admin on Fri Dec 15 18:25:55 GMT 2023 , Edited by admin on Fri Dec 15 18:25:55 GMT 2023
PRIMARY
MESH
C008385
Created by admin on Fri Dec 15 18:25:55 GMT 2023 , Edited by admin on Fri Dec 15 18:25:55 GMT 2023
PRIMARY
PUBCHEM
31368
Created by admin on Fri Dec 15 18:25:55 GMT 2023 , Edited by admin on Fri Dec 15 18:25:55 GMT 2023
PRIMARY
HSDB
5613
Created by admin on Fri Dec 15 18:25:55 GMT 2023 , Edited by admin on Fri Dec 15 18:25:55 GMT 2023
PRIMARY
CAS
126-98-7
Created by admin on Fri Dec 15 18:25:55 GMT 2023 , Edited by admin on Fri Dec 15 18:25:55 GMT 2023
PRIMARY
EPA CompTox
DTXSID1024176
Created by admin on Fri Dec 15 18:25:55 GMT 2023 , Edited by admin on Fri Dec 15 18:25:55 GMT 2023
PRIMARY
NSC
24145
Created by admin on Fri Dec 15 18:25:55 GMT 2023 , Edited by admin on Fri Dec 15 18:25:55 GMT 2023
PRIMARY
WIKIPEDIA
METHACRYLONITRILE
Created by admin on Fri Dec 15 18:25:55 GMT 2023 , Edited by admin on Fri Dec 15 18:25:55 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-817-5
Created by admin on Fri Dec 15 18:25:55 GMT 2023 , Edited by admin on Fri Dec 15 18:25:55 GMT 2023
PRIMARY